用于异相芬顿处理的氧化锰:催化剂还是抑制剂?

Jianfeng Zheng, Hyun Jeong Lim, Tayler Hedtke, Jae-Hong Kim, Shuo Zhang
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引用次数: 0

摘要

氧化锰物种经常被用于芬顿催化剂的设计,但它们在与过氧化氢(HO)反应中的作用仍存在争议。我们在此揭示了氧化锰/过氧化氢在大块表面与纳米孔封闭表面发生相互作用的不同途径,而这一点在文献中一直被忽视。简而言之,颗粒状氧化锰受锰的价数和溶液pH值的影响会导致HO快速分解,但不会产生用于水处理的活性氧(OH、O或O);相反,纳米孔(1 nm)中氧化锰/HO的相互作用会产生自由基(主要是OH和O)并去除有机污染物。我们通过实验和计算研究深入了解了不同的反应路线。我们的研究结果提醒人们在开发芬顿催化剂时不要一味追求锰,以免造成 HO 分解失效和自由基生成缓慢。
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Manganese oxide for heterogeneous Fenton treatment: Catalyst or inhibitor?
Manganese oxide species have been frequently used for Fenton catalyst design, but their role in reaction with hydrogen peroxide (HO) is still in debate. We here revealed the different routes of manganese oxide/HO interactions occurring at bulk surfaces to that at nanopore-confined surfaces, which have been overlooked in literatures. Briefly, particulate manganese oxide species cause a fast HO decomposition influenced by the valence of manganese and solution pH, but without generation of reactive oxygen species (OH, O, or O) for water treatment; in contrast, manganese oxide/HO interaction under nanopore confinement ( 1 nm) led to the production of radicals (mainly OH and O) and the removal of organic pollutants. We gained insights into the differed reaction routes based on experimental and computational study. Our findings provide caveats on the indiscriminate pursuit of manganese in Fenton catalyst development, against a nullified HO decomposition and impractically slow radical production.
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